Literature DB >> 8616788

Trisomy 21 in solitary fibrous tumor.

P Dal Cin1, R Sciot, C D Fletcher, C Hilliker, I De Wever, B Van Damme, H Van den Berghe.   

Abstract

We found trisomy 21 as the sole chromosome abnormality in a solitary fibrous tumor arising at a nonpleural site. No cytogenetic investigation of solitary fibrous tumors has previously been reported.

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Year:  1996        PMID： 8616788     DOI： 10.1016/0165-4608(95)00179-4

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN： 0165-4608


  4 in total

1.  Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group.

Authors:  C D Fletcher; P Dal Cin; I de Wever; N Mandahl; F Mertens; F Mitelman; J Rosai; A Rydholm; R Sciot; G Tallini; H van den Berghe; R Vanni; H Willén
Journal:  Am J Pathol       Date:  1999-06       Impact factor: 4.307

2.  Solitary fibrous tumor with entrapment of minor salivary gland tissue: an unusual presentation that requires exclusion of pleomorphic adenoma.

Authors:  Jose Luis Tapia; Samuel Goodloe; Joseph E Margarone; Michael R Markiewicz; Alfredo Aguirre
Journal:  Head Neck Pathol       Date:  2011-03-19

3.  Lack of a common or characteristic cytogenetic anomaly in solitary fibrous tumor.

Authors:  Alireza Torabi; Subodh M Lele; Dominick DiMaio; Jeffrey C Pinnt; Michelle M Hess; Marilu Nelson; Julia A Bridge
Journal:  Cancer Genet Cytogenet       Date:  2008-02

Review 4.  The many faces of solitary fibrous tumor; diversity of histological features, differential diagnosis and role of molecular studies and surrogate markers in avoiding misdiagnosis and predicting the behavior.

Authors:  Muhammad Usman Tariq; Nasir Ud Din; Jamshid Abdul-Ghafar; Yong-Koo Park
Journal:  Diagn Pathol       Date:  2021-04-20       Impact factor: 2.644
  4 in total

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